Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 50692013 | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484534018 | Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 761274013 | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1216334015 | HHH - Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1217833013 | HHH - Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | Is a | Hyperammonemia | true | Inferred relationship | Existential restriction modifier | ||
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | Is a | Disorder of ornithine metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | Is a | Hyperornithinemia | true | Inferred relationship | Existential restriction modifier | ||
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR